EVERWIN GLOBAL LANGUAGE
The Leading Globalization Services Provider
LIFE SCIENCES SOLUTIONS
Gain greater process efficiency, reduce translation costs, and speed up go-to-market with our specialized language and content solutions across life sciences, medical research, and contract research organizations (CROs).
Now you can create real value for your teams and ecosystem partners to drive better outcomes for scientists, medical representatives, professionals, and patients alike.
WHY EGL ?
Address scalability, accuracy, quality, and compliance across the value chain with an organization you can trust.
HELPING 3 OF THE 20 TOP MEDICAL DEVICE COMPANIES.
WORKING WITH 3 OF THE TOP 30 CLINICAL RESEARCH ORGANIZATIONS.
2,000+ IN-HOUSE LINGUISTS.
24/7/365 SUPPORT ACROSS THE GLOBE.
AREAS OF EXPERTISE
Comprehensive content and language solutions for the Life Sciences industry.
BIOTECHNOLOGY
Translate your clinical trial, regulatory, manufacturing, and legal documentation, as well as marketing communications with repeatable quality.
MEDICAL DEVICES
Expert localization across product content, documentation, and software for a versatile and personalized approach to healthcare.
CLINICAL RESEARCH ORGANIZATIONS (CRO)
End-to-end linguistic solutions for the full lifecycle of clinical development, from discovery and product development to regulatory submission and commercialization.
PHARMACEUTICAL
Fast, flexible, and cost-effective language solutions for time-critical documentation such as clinical trials, submissions, or product launches.
ANIMAL HEALTH
Specialized multilingual support for health policies, protocols, research, labeling, marketing material, scientific articles, and veterinary expert reports.
MANAGED HEALTHCARE
Transform your content into multilingual, multi-accessible material to drive more patient value for all, across all customer touchpoints.
OUR SOLUTIONS
MANAGE MULTILINGUAL REGULATORY LABELING & SUBMISSIONS
Streamline complex labeling requirements and maintain accurate product information globally.
Our solution enables you to capture and track label changes, reuse regulated-approved translations, simplify the review process, as well as lower the cost of translation workload.
TRANSLATE GLOBAL CLINICAL TRIAL DOCUMENTS
Establish a scalable translation model that can adhere to the milestone requirements, from clinical trial study start-ups to regulatory submissions. We can help facilitate through all phases of your clinical trial, covering file preparation, translation and review, desktop publishing, and quality assurance.
SECURE THE TRANSLATION SUPPLY CHAIN
Increase the efficiency of projects with technology-enabled translations choosing from a full range of deployment options to streamline your localization projects.
Our technology is secure by design and our quality processes are based on our deep understanding of the regulations involved—including FDA, MHRA, and MHLW—so you can have peace of mind for all of your regulated content.
MANAGE REGULATORY COMPLIANCE DOCUMENT DEMANDS
If you are still using traditional methods of documentation, delivering high-quality, timely publications can be challenging.
Adopt a centralized knowledge hub to align teams, create a robust translation, and review processes—including oversight and audit tracking—drive content reuse, and promote standardization so you can speed up content changes.
